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顯示項目 255391-255400 / 2346260 (共234626頁)
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| 臺大學術典藏 |
2021-11-22T02:27:28Z |
Chromosomal polymorphism of ribosomal genes in the genus Oryza
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Chung, M.-C.; Lee, Y.-I.; Cheng, Y.-Y.; Chou, Y.-J.; Lu, C.-F. |
| 中國醫藥大學 |
2013-04 |
Chromosome 10q Deletion del (10)(q26.1q26.3) is Associated with Cataract
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張鈺孜(chang, yu-tzu);Chou), 周宜卿(I-Ching;Wang), 王仲興(Chung-Hsing;Chin), 陳震南(Zheng-Nan;Kuo), 郭煌宗(Haung-Tsung;Lin), 林齊強(Chyi-Chyang;Tsai), 蔡長海(Chang-Hai;Tsai)*, 蔡輔仁(Fuu-Jen |
| 亞洲大學 |
2011-09 |
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3)
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陳持平;Chen, Chih-Ping;Li-Feng Chen, ;Adam Hwa-Ming Hsieh, ;Wang, Wayseen |
| 中國醫藥大學 |
2011-09 |
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3)
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陳持平(Chih-Ping Chen)*;(Yi-Hui Lin);(Heng-Kien Au);(Chin-Yuan Hsu);(Yu-Peng Liu);(Pei-Chen Wu);(Schu-Rern Chern);(Yu-Ting Chen);(Li-Feng Chen);(Adam Hwa-Ming Hsieh);(Wayseen Wang) |
| 國立交通大學 |
2014-12-08T15:23:14Z |
Chromosome 15q21-22-Related Polymorphisms and Haplotypes Are Associated with Susceptibility to Type-2 Diabetic Nonproliferative Retinopathy
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Hsieh, Yao-Yuan; Huang, Yu-Chuen; Chang, Chi-Chen; Wang, Yu-Kuo; Lin, Wen-Hsin; Tsai, Fuu-Jen |
| 中國醫藥大學 |
2012-05 |
Chromosome 15q21-22-related polymorphisms and haplotypes are associated with susceptibility to type-2 diabetic nonproliferative retinopathy
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謝耀元(Hsieh Yao-Yuan);黃毓銓(Yu-Chuen Huang);(Chi-Chen Chang);(Yu-Kuo Wang);林文鑫(Wen-Hsin Lin);蔡輔仁(Fuu-Jen Tsai)* |
| 中國醫藥大學 |
2013-12 |
Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review
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陳持平(Chih-Ping Chen)*;(Tung-Yao Chang);(Wan-Yuo Guo);(Pei-Chen Wu);(Liang-Kai Wang);(Schu-Rern Chern);(Peih-Shan Wu);蘇俊維(Jun-Wei Su);(Yu-Ting Chen);(Li-Feng Chen);(Wayseen Wang) |
| 亞洲大學 |
201309 |
Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes
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陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 臺大學術典藏 |
2018-09-10T06:00:32Z |
Chromosome 1p aberrations are frequent in human primary hepatocellular carcinoma
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Chen, H.-L., Chen, Y.-C., Chen, D.-S.; Hui-Ling Chen; DING-SHINN CHEN |
| 中國醫藥大學 |
2011-09 |
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia
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陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Yi-Yung Chen);(Schu-Rern Chern);(Yu-Peng Liu);(Pei-Chen Wu);(Chen-Chi Lee);(Yu-Ting Chen);(Wayseen Wang) |
顯示項目 255391-255400 / 2346260 (共234626頁)
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